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Who was studied 405,540 European ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.00791 lower (95% confidence interval 0.0054-0.0104); p = 8 × 10−10.
How common The G allele had a frequency of about 51% in the people studied.
Where it sits Chromosome 5, band 5p12 — inside ANXA2R-OT1.
What each result means
G/GTwo copies of the version the research linked to Height (baseline). That is the strongest link of the three results. A link in a study is not a diagnosis.
G/TOne copy of the version the research linked to Height (baseline). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Height (baseline). This is the starting point the study compared everyone against.
Nature communications · 2025 · PMID 40374629 · open access
Questions about rs12187928
What is rs12187928?
rs12187928 is a single position in the genome, in or near the ANXA2R-OT1 gene. Published research associates it with height (baseline). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs12187928 linked to?
On MyGeneLog this position is linked to Height. The research behind each link, and its sources, are set out on that condition page.
Does having rs12187928 mean I will get this?
No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.
Where does the information about rs12187928 come from?
GWAS Catalog, Nature communications 2025, PMID:40374629. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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